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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368141Generated: November 1, 2026

Sodium borohydride → HCID 178472351, compound

https://huagongshe.com/reaction/2368141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178472350HCID 178472350—
SolventEthanolHCID 702—
ProductHCID 178472351HCID 178472351104%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-({trans-4-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]cyclohexyl}oxy)propan-2-one (259 mg) in ethanol (5 mL) was added sodium borohydride (57 mg) under ice-cooling. The reaction mixture was stirred at 0° C. for 1 hr, and extracted with ethyl acetate and 1M hydrochloric acid. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (271 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-d7c7451cd7364109987354ffd1a4c7ef
Source noteuspto-grants-2014_04